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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766381Generated: November 1, 2026

Vinyl benzoate → Acetate

https://huagongshe.com/reaction/1766381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl benzoateHCID 13037—
Reactant2-(3-(Di(propan-2-yl)amino)-1-phenylpropyl)-4-(hydroxymethyl)phenolHCID 9927971—
Solventtert-Butyl methyl etherHCID 15413—
ProductAcetateHCID 175—
ProductFormateHCID 283—
ProductButyrateHCID 104775—

Reaction Steps

A mixture consisting of Intermediate B (80 mg, 0.23 mmol), vinyl ester (0.4 ml), tert.-butyl methylether (18 ml), and lipase enzyme (1.0 g) was gently shaken at room temperature. Benzylic formate, acetate, and n-butyrate were prepared from the corresponding vinyl ester donors using SAM I lipase (Amano Pharmaceutical Co.). Benzoylation was achieved with vinyl benzoate in the presence of Lipozym IM 20 (Novo Nordisk), whereas pivalates and isobutyrates were obtained from the corresponding vinyl esters under catalysis of Novozym SP 435 (Novo Nordisk). Tlc analysis indicated after 2-24 hrs complete disappearence of the starting material (Rf=0.45 (3)). The mixture was filtered and then evaporated under high vacuum (<40° C.) to give the carboxylic acid (R1—CO2H) salts of the respective benzylic monoesters as colourless to light yellow oils.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230030B2
Source datasetuspto-grants-2007_06
ORD IDord-9aebc1dadfc04bc39058aa15aa8153c3
Source noteuspto-grants-2007_06